Xie X, Gerber U, Gähwiler B H, Smart T G
Department of Pharmacology, School of Pharmacy, London, UK.
Neurosci Lett. 1993 Sep 3;159(1-2):46-50. doi: 10.1016/0304-3940(93)90795-m.
The actions of zinc on ionotropic and metabotropic glutamate receptors were studied using intracellular recording in acutely prepared adult rat hippocampal slices and in organotypic hippocampal slice cultures. In control Krebs, glutamate and non-N-methyl-D-aspartate (NMDA) agonist-induced responses were enhanced by zinc (25-300 microM). However, under conditions favouring NMDA receptor activation, zinc inhibited glutamate- and NMDA-induced responses. Metabotropic glutamate receptor-mediated responses activated in cultured slices by 1-amino-cyclopentane-1,3-dicarboxylate (1S,3R-ACPD) or by quisqualate, were reversibly inhibited by zinc (200 microM). These results indicate that zinc can inhibit responses induced by activation of metabotropic glutamate receptors and reaffirm that zinc has a differential effect on NMDA and non-NMDA receptors.
利用急性制备的成年大鼠海马切片和海马脑片培养物中的细胞内记录技术,研究了锌对离子型和代谢型谷氨酸受体的作用。在对照的 Krebs 溶液中,锌(25 - 300微摩尔)增强了谷氨酸和非N - 甲基 - D - 天冬氨酸(NMDA)激动剂诱导的反应。然而,在有利于NMDA受体激活的条件下,锌抑制了谷氨酸和NMDA诱导的反应。在培养的脑片中,由1 - 氨基 - 环戊烷 - 1,3 - 二羧酸(1S,3R - ACPD)或喹啉酸激活的代谢型谷氨酸受体介导的反应,被锌(200微摩尔)可逆性抑制。这些结果表明,锌可以抑制代谢型谷氨酸受体激活所诱导的反应,并再次证实锌对NMDA和非NMDA受体具有不同的作用。